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Difficulty of diagnosing Wegener's granulomatosis in the head and neck region

✍ Scribed by Kenzo Tsuzuki; Keijiro Fukazawa; Hironori Takebayashi; Kengo Hashimoto; Masafumi Sakagami


Book ID
116223548
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
692 KB
Volume
36
Category
Article
ISSN
0385-8146

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## Abstract Wegener's granulomatosis (WG) is one type of systemic small vessel vasculitis and antineutrophil cytoplasmic antibodies (ANCA) have become an established diagnostic tool for systemic vasculitis. The sensitivity and specificity of anti‐PR3 (proteinase 3) capture enzyme‐linked immunosorbe